Canonical Allele Identifier: CA1882682452

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133456138G= , CM000671.2:g.133456138G=	GRCh38
NC_000009.10:g.135311081G=	NCBI36
NG_011934.2:g.46800G= , LRG_544:g.46800G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3470G= MANE Select	ENSP00000347927.2:p.Cys1157=
ENST00000355699.6:c.3470G=	ENSP00000347927.2:p.Cys1157=
ENST00000356589.6:c.3377G=	ENSP00000348997.2:p.Cys1126=
ENST00000371910.1:c.26G=	ENSP00000360978.1:p.Cys9=
ENST00000371916.5:c.*939G=	ENSP00000360984.2:n.*939G=
ENST00000371929.7:c.3638G=	ENSP00000360997.3:p.Cys1213=
ENST00000485925.5:n.2286G=
NM_139025.4:c.3638G= , LRG_544t1:c.3638G=	NP_620594.1:p.Cys1213=
NM_139026.4:c.3377G=	NP_620595.1:p.Cys1126=
NM_139027.4:c.3470G=	NP_620596.2:p.Cys1157=
NR_024514.2:n.2305G=
XM_011518174.1:c.3248G=	XP_011516476.1:p.Cys1083=
XM_011518175.1:c.*45G=	XP_011516477.1:n.*45G=
XM_011518176.1:c.2654G=	XP_011516478.1:p.Cys885=
XM_011518177.1:c.2648G=	XP_011516479.1:p.Cys883=
XM_011518178.1:c.2303G=	XP_011516480.1:p.Cys768=
XM_011518179.1:c.2303G=	XP_011516481.1:p.Cys768=
XM_011518180.1:c.1904G=	XP_011516482.1:p.Cys635=
XM_011518176.3:c.2654G=	XP_011516478.1:p.Cys885=
XM_011518178.2:c.2303G=	XP_011516480.1:p.Cys768=
XM_017014232.1:c.3626G=	XP_016869721.1:p.Cys1209=
XM_017014233.1:c.3248G=	XP_016869722.1:p.Cys1083=
XM_017014234.2:c.2648G=	XP_016869723.1:p.Cys883=
NM_139026.5:c.3377G=	NP_620595.1:p.Cys1126=
NM_139027.5:c.3470G=	NP_620596.2:p.Cys1157=
NM_139025.5:c.3638G=	NP_620594.1:p.Cys1213=
NM_139026.6:c.3377G=	NP_620595.1:p.Cys1126=
NM_139027.6:c.3470G= MANE Select	NP_620596.2:p.Cys1157=
NR_024514.3:n.2307G=